Syntara relata feedback positivo da FDA sobre o estudo do amsulostat

A Syntara Limited realizou um webinar para acionistas em 29 de abril para discutir o feedback da FDA sobre sua proposta de estudo de Fase IIb para o amsulostat no tratamento de mielofibrose, além de um aumento de capital e o relatório trimestral. O CEO Gary Phillips destacou o caminho acordado com os órgãos reguladores. A empresa protocolou seu relatório trimestral Appendix 4C na ASX.

A Syntara Limited (PMXSF) conduziu um webinar para investidores e uma sessão de perguntas e respostas em 29 de abril, às 21h (horário de verão do leste dos EUA), após anúncios importantes. O CEO Gary Phillips, médico e diretor, apresentou atualizações sobre o principal ativo, o amsulostat, as interações com a FDA, o aumento de capital e o último relatório trimestral de fluxo de caixa protocolado na ASX como Appendix 4C. Matthew Wright conduziu a chamada, apresentando Phillips para abordar diretamente os interesses dos investidores. Gary Phillips enfatizou a análise positiva da FDA sobre o amsulostat, baseada nos dados da Fase II relatados no ano passado. A agência concordou com um caminho a seguir para o estudo de Fase IIb em mielofibrose, o que Phillips descreveu como significativo para os acionistas e para os próximos passos da empresa. O aumento de capital inclui uma colocação de US$ 8 milhões, elevando o caixa pro forma para US$ 16,9 milhões, excluindo quaisquer receitas do Plano de Compra de Ações. Phillips observou que isso posiciona a Syntara até o terceiro trimestre. Os investidores participaram através de instruções do operador para perguntas ao final.

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